Classifications

• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
  • B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
  • B41M5/00—Duplicating or marking methods; Sheet materials for use therein
  • B41M5/50—Recording sheets characterised by the coating used to improve ink, dye or pigment receptivity, e.g. for ink-jet or thermal dye transfer recording
  • B41M5/52—Macromolecular coatings
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
  • B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
  • B41M5/00—Duplicating or marking methods; Sheet materials for use therein
  • B41M5/50—Recording sheets characterised by the coating used to improve ink, dye or pigment receptivity, e.g. for ink-jet or thermal dye transfer recording
  • B41M5/502—Recording sheets characterised by the coating used to improve ink, dye or pigment receptivity, e.g. for ink-jet or thermal dye transfer recording characterised by structural details, e.g. multilayer materials
  • B41M5/506—Intermediate layers
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
  • B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
  • B41M5/00—Duplicating or marking methods; Sheet materials for use therein
  • B41M5/50—Recording sheets characterised by the coating used to improve ink, dye or pigment receptivity, e.g. for ink-jet or thermal dye transfer recording
  • B41M5/502—Recording sheets characterised by the coating used to improve ink, dye or pigment receptivity, e.g. for ink-jet or thermal dye transfer recording characterised by structural details, e.g. multilayer materials
  • B41M5/508—Supports
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
  • B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
  • B41M5/00—Duplicating or marking methods; Sheet materials for use therein
  • B41M5/50—Recording sheets characterised by the coating used to improve ink, dye or pigment receptivity, e.g. for ink-jet or thermal dye transfer recording
  • B41M5/52—Macromolecular coatings
  • B41M5/5218—Macromolecular coatings characterised by inorganic additives, e.g. pigments, clays
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
  • B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
  • B41M5/00—Duplicating or marking methods; Sheet materials for use therein
  • B41M5/50—Recording sheets characterised by the coating used to improve ink, dye or pigment receptivity, e.g. for ink-jet or thermal dye transfer recording
  • B41M5/52—Macromolecular coatings
  • B41M5/5236—Macromolecular coatings characterised by the use of natural gums, of proteins, e.g. gelatins, or of macromolecular carbohydrates, e.g. cellulose
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
  • B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
  • B41M5/00—Duplicating or marking methods; Sheet materials for use therein
  • B41M5/50—Recording sheets characterised by the coating used to improve ink, dye or pigment receptivity, e.g. for ink-jet or thermal dye transfer recording
  • B41M5/52—Macromolecular coatings
  • B41M5/5245—Macromolecular coatings characterised by the use of polymers containing cationic or anionic groups, e.g. mordants
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
  • B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
  • B41M5/00—Duplicating or marking methods; Sheet materials for use therein
  • B41M5/50—Recording sheets characterised by the coating used to improve ink, dye or pigment receptivity, e.g. for ink-jet or thermal dye transfer recording
  • B41M5/52—Macromolecular coatings
  • B41M5/5254—Macromolecular coatings characterised by the use of polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds, e.g. vinyl polymers
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
  • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
  • Y10T428/00—Stock material or miscellaneous articles
  • Y10T428/31504—Composite [nonstructural laminate]
  • Y10T428/31725—Of polyamide
  • Y10T428/31768—Natural source-type polyamide [e.g., casein, gelatin, etc.]
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
  • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
  • Y10T428/00—Stock material or miscellaneous articles
  • Y10T428/31504—Composite [nonstructural laminate]
  • Y10T428/31725—Of polyamide
  • Y10T428/31768—Natural source-type polyamide [e.g., casein, gelatin, etc.]
  • Y10T428/31772—Next to cellulosic
  • Y10T428/31775—Paper
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
  • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
  • Y10T428/00—Stock material or miscellaneous articles
  • Y10T428/31504—Composite [nonstructural laminate]
  • Y10T428/31725—Of polyamide
  • Y10T428/31779—Next to cellulosic
  • Y10T428/31783—Paper or wood
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
  • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
  • Y10T428/00—Stock material or miscellaneous articles
  • Y10T428/31504—Composite [nonstructural laminate]
  • Y10T428/31855—Of addition polymer from unsaturated monomers

Definitions

• the present invention relates to an ink jet image-recording element which yields printed images with excellent image stability over a wide range of humidity conditions.
• ink droplets are ejected from a nozzle at high speed towards a recording element or medium to produce an image on the medium.
• the ink droplets, or recording liquid generally comprise a recording agent, such as a dye or pigment, and a large amount of solvent.
• the solvent, or carrier liquid typically is made up of water, an organic material such as a monohydric alcohol, a polyhydric alcohol or mixtures thereof.
• An ink jet recording element typically comprises a support having on at least one surface thereof an ink-receiving or image-recording layer, and includes those intended for reflection viewing, which have an opaque support, and those intended for viewing by transmitted light, which have a transparent support.
• Medical images such as radiographic images, are typically viewed on a blue transparent support.
• an ink jet recording element must:
• Image stability is an important concern for inkjet prints.
• dyes used in the printing process may continue to migrate over time during storage of a printed image.
• the migration process typically occurs more quickly under conditions of high relative humidity since inkjet dyes are water soluble and materials used to manufacture inkjet media are often easily plasticized by water.
• the individual dyes may migrate or bleed at different rates due to differences in solubility or molecular dimensions.
• areas which are originally printed as neutral densities may acquire a colored tint over time.
• Such a phenomenon is especially objectionable in a medical application such as a radiographic image, since a neutral gray scale is expected and a colored tint is typically unacceptable in any area of the print.
• U.S. Pat. No. 4,547,405 relates to an ink jet receiver comprising an ink jet recording layer which contains a polymeric latex of a block copolymer of polyvinyl alcohol and polyvinyl (benzyl ammonium chloride).
• a polymeric latex of a block copolymer of polyvinyl alcohol and polyvinyl (benzyl ammonium chloride) contains a polymeric latex of a block copolymer of polyvinyl alcohol and polyvinyl (benzyl ammonium chloride).
• an ink jet recording element comprising a support having thereon an image-recording layer comprising a binder and a polymeric mordant, the image-recording layer providing a total concentration of charged polymeric binding sites greater than about 3 ⁇ 10 26 /m 3 , and the image-receiving layer having a concentration of salts providing charges, opposite to the charge of the binding sites, of less than about 5.8 ⁇ 10 26 charges/m 3 , the salt having a molecular weight of less than 10,000 grams/mole.
• an image can be produced which has improved image stability under high humidity conditions.
• the concentration of salts providing charges, opposite to the charge of said binding sites is less than about 1.0 ⁇ 10 26 charges/m 3 . In another preferred embodiment of the invention, the concentration of salts providing charges, opposite to the charge of said binding sites, is less than about 5.0 ⁇ 10 24 charges/m 3 .
• Any polymeric mordant can be used in the image-recording layer of the invention provided it has the binding site concentration noted above.
• a cationic polymer e.g., a polymeric quartenary ammonium compound, or a basic polymer, such as poly(dimethylaminoethyl)-methacrylate, polyalkylenepolyamines, and products of the condensation thereof with dicyanodiamide, amine-epichlorohydrin polycondensates; lecithin and phospholipid compounds.
• mordants useful in the invention include: vinylbenzyl trimethyl ammonium chloride/ethylene glycol dimethacrylate; vinylbenzyl trimethyl ammonium chloride/divinyl benzene; poly(diallyl dimethyl ammonium chloride); poly(2-N,N,N-trimethylammonium)ethyl methacrylate methosulfate; poly(3-N,N,N-trimethylammonium)propyl methacrylate chloride; a copolymer of vinylpyrrolidinone and vinyl(N-methylimidazolium chloride; and hydroxyethylcellulose derivitized with (3-N,N,N-trimethylammonium) propyl chloride.
• the mordant is a polymeric quaternary ammonium compound.
• impurities may be introduced in the form of salts.
• the source of these salts include the starting reagents, by-products of pH adjustment and undesired side reactions. It has been found that when the amount of these salts is reduced to a certain level, then improved image stability under high humidity conditions can be obtained.
• the binder is a hydrophilic material.
• hydrophilic materials include naturally-occurring hydrophilic colloids and gums such as gelatin, albumin, guar, xantham, acacia, chitosan, starches and their derivatives, functionalized proteins, functionalized gums and starches, and cellulose ethers and their derivatives, polyvinyloxazoline and polyvinylmethyloxazoline, polyoxides, polyethers, poly(ethylene imine), poly(acrylic acid), poly(methacrylic acid), n-vinyl amides including polyacrylamide and polyvinylpyrrolidone, and poly(vinyl alcohol), its derivatives and copolymers.
• the hydrophilic binder is gelatin.
• the hydrophilic material which may be employed in the image-recording layer may be present in any amount which is effective for the intended purpose. In general, it may be present in an amount of from about 0.5 to about 20 g/m 2 , which corresponds to a dry thickness of about 0.5 to about20 ⁇ m.
• the void volume must be sufficient to absorb all of the printing ink. For example, if a porous layer has 60 volume % open pores, in order to absorb 32 cc/m 2 of ink, it must have a physical thickness of 54 ⁇ m.
• Matte particles may be added to any or all of the layers described in order to provide enhanced printer transport, or resistance to ink offset.
• surfactants, defoamers, or other coatability-enhancing materials may be added as required by the coating technique chosen.
• Crosslinkers may also be added to the layers in order to impart improved mechanical properties or resistance to dissolution.
• Any support or substrate may be used in the recording element of the invention.
• polyethylene-coated paper or poly(ethylene terephthalate) is preferred.
• the support is suitably of a thickness of from about 50 to about 500 ⁇ m, preferably from about 75 to 300 ⁇ m.
• Antioxidants, antistatic agents, plasticizers, dyes, pigments and other known additives may be incorporated into the support, if desired.
• the surface of the support may be subjected to a corona-discharge treatment prior to applying the image-recording layer.
• an additional backing layer or coating may be applied to the backside of a support (i.e., the side of the support opposite the side on which the image-recording layers are coated) for the purposes of improving the machine-handling properties and curl of the recording element, controlling the friction and resistivity thereof, and the like.
• the backing layer may comprise a binder and a filler.
• Typical fillers include amorphous and crystalline silicas, poly(methyl methacrylate), hollow sphere polystyrene beads, micro crystalline cellulose, zinc oxide, talc, and the like.
• the filler loaded in the backing layer is generally less than 5 percent by weight of the binder component and the average particle size of the filler material is in the range of 5 to 30 ⁇ m.
• Typical binders used in the backing layer are polymers such as acrylates, gelatin, methacrylates, polystyrenes, acrylamides, poly(vinyl chloride)poly(vinyl acetate) co-polymers, poly(vinyl alcohol), cellulose derivatives, and the like.
• an antistatic agent also can be included in the backing layer to prevent static hindrance of the recording element.
• Particularly suitable antistatic agents are compounds such as dodecylbenzenesulfonate sodium salt, octyl-sulfonate potassium salt, oligostyrenesulfonate sodium salt, laurylsulfosuccinate sodium salt, and the like.
• the antistatic agent may be added to the binder composition in an amount of 0.1 to 15 percent by weight, based on the weight of the binder.
• An image-recording layer may also be coated on the backside, if desired.
• the hydrophilic film forming binders described above may also include a crosslinker.
• a crosslinker such as carbodiimides, polyfunctional aziridines, melamine formaldehydes, isocyanates, epoxides, and the like may be used. If a crosslinker is added, care must be taken that excessive amounts are not used as this will decrease the swellability of the layer, reducing the drying rate of the printed areas.
• Coating compositions employed in the invention may be applied by any number of well known techniques, including dip-coating, wound-wire rod coating, doctor blade coating, gravure and reverse-roll coating, slide coating, bead coating, extrusion coating, curtain coating and the like.
• Known coating and drying methods are described in further detail in Research Disclosure no. 308119, published Dec. 1989, pages 1007 to 1008.
• Slide coating is preferred, in which the base layers and overcoat may be simultaneously applied. After coating, the layers are generally dried by simple evaporation, which may be accelerated by known techniques such as convection heating.
• the ink jet inks used to image the recording elements of the present invention are well-known in the art.
• the ink compositions used in ink jet printing typically are liquid compositions comprising a solvent or carrier liquid, dyes or pigments, humectants, organic solvents, detergents, thickeners, preservatives, and the like.
• the solvent or carrier liquid can be solely water or can be water mixed with other water-miscible solvents such as polyhydric alcohols.
• Inks in which organic materials such as polyhydric alcohols are the predominant carrier or solvent liquid may also be used. Particularly useful are mixed solvents of water and polyhydric alcohols.
• the dyes used in such compositions are typically water-soluble direct or acid type dyes.
• Such liquid compositions have been described extensively in the prior art including, for example, U.S. Pat. Nos. 4,381,946; 4,239,543 and 4,781,758, the disclosures of which are hereby incorporated by reference.
• Pen plotters operate by writing directly on the surface of a recording medium using a pen consisting of a bundle of capillary tubes in contact with an ink reservoir.
• a comparison element C-1 was prepared which did not contain any mordant. All of the mordants were dialyzed or diafiltered with the intention of removing ions. The samples that were dialyzed were purified with a membrane manufactured by Spectrum Medical Industries, Inc. having a nominal molecular weight cutoff of 12,000 to 14,000 g/mole. The diafiltered sample was purified using a diafiltration membrane manufactured by Osmonics Inc. with a nominal molecular weight cutoff of 20,000 g/mole.
• the mordants were characterized for salt content by ion chromatography.
• the analytical method excludes molecules with molecular weights greater than 10,000 g/mole. Since the most common anion by a wide margin in all cases is chloride, this is reported in the table below as impurity charge.
• the impurity charge reported below reflects only chloride associated with molecules having molecular weights below 10,000 g/mole.
• Each of the mordants listed should normally contain some chlorine present as a counterion to the mordanting cationic groups, but the level measured was sufficiently high that it may be safely assumed that the levels measured are generally far in excess of any expected amount.
• Each mordant was combined with photographic grade bone gelatin (Eastman Gelatine Co.) in deionized water to make a solution at 10% solids. The weight ratio of gelatin to mordant in every case was 75:25.
• Each melt was then bead coated on resin-coated paper which had been corona-discharge treated to improve adhesion. Simultaneously, an overcoat was applied from a 2% solids solution of methyl cellulose, Methocel A4C ®,(Dow Chemical Co.). The coated element was chill set at 5° C. and dried thoroughly by forced air heating. The final dry coverage of the gelatin/mordant base layer was 12.9 g/m 2 ; and the dry coverage of the overcoat was 0.81 g/m 2 .
• a gray scale image was printed on each receiver using an Eastman Kodak 1200 Distributed Medical Imager. The image was allowed to dry under ambient office conditions and then incubated at 80% relative humidity, 21° C. for 72 hours. The cyan, magenta and yellow optical densities were measured at various neutral densities of 0.4, 0.7 and 1.3, before and after incubation, and the % increase for each calculated. The % increase in optical density is a convenient measure of the amount of dye migration for each of the dyes used to compose the image. An average of the increase in optical density at the three neutral densities was measured as follows:
• the bottommost ink absorbing layer comprised 7.5 g/m 2 deionized photographic grade pigskin gelatin (SBI)
• the middle dye mordanting layer comprised 7.5 g/m 2 of a combination of the same gelatin with the above described mordant
• the topmost overcoat comprised 0.54 g/m 2 methyl cellulose, Methocel A4C®, (Dow Chemical Co.)
• Gelatin/mordant weight ratios for the middle layer were 90/10, 80/20, and 70/30. From this information, the effective mordant (cationic groups) concentration per unit volume of the coated film was calculated and is reported as mordant charge per cubic meter.
• a gray scale image was printed on each element using an Eastman Kodak 3600 Distributed Medical Imager.
• the elements were as tested as above with the following results:

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• Ink Jet Recording Methods And Recording Media Thereof (AREA)
• Laminated Bodies (AREA)
• Compositions Of Macromolecular Compounds (AREA)
• Ink Jet (AREA)

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• 1999
  • 1999-09-13 US US09/394,420 patent/US6303212B1/en not_active Expired - Lifetime
• 2000
  • 2000-09-01 EP EP00203046A patent/EP1084857B1/de not_active Expired - Lifetime
  • 2000-09-01 DE DE60008657T patent/DE60008657T2/de not_active Expired - Fee Related
  • 2000-09-13 JP JP2000277629A patent/JP2001121808A/ja active Pending

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